Implantable end pad

ABSTRACT

Disclosed is an implantable end pad. The end pad includes a bone attachment portion having a recess configured to receive an amputated bone of a residual limb. The end pad further includes an end portion having a contour corresponding to at least a portion of a socket of an artificial limb such that the end pad can be at least partially received in the socket of the residual limb. Further disclosed is a method wherein the end pad is implanted into a residual limb by way of a surgical procedure.

RELATED APPLICATIONS

This application claims the benefit of U.S. Provisional Application No. 61/498,670, filed 20 Jun. 2011, the entirety of which is herein incorporated by reference.

BACKGROUND

This disclosure relates to an implantable end pad that helps secure an artificial limb to a residual limb of an amputee.

Artificial, or prosthetic, limbs are typically used to replace parts lost by injury. Artificial limbs are known to include sockets sized to receive an amputee's residual limb.

FIG. 1 is representative of a typical residual limb 1, including an amputated bone 2 and various soft tissue 4. In the prior art, an artificial limb 6 may be custom fit for the residual limb 1, such that the socket 8 is sized to receive the residual limb 1. The residual limb 1 may be a leg amputated below or above the knee, or an arm amputated below or above the elbow, as examples. The artificial limb 6 is selected to correspond to the particular residual limb 1 and to provide a desired level of performance. The residual limb 1 may be fit with a liner or other interface to provide padding between the residual limb 1 and the socket 8. The liner may be positioned within the socket 8 between the soft tissue 4 and the artificial limb 6.

SUMMARY

Disclosed is an implantable end pad. The end pad includes a bone attachment portion having a recess configured to receive an amputated bone of a residual limb. The end pad further includes an end portion having a contour corresponding to at least a portion of a socket of an artificial limb such that the end pad can be at least partially received in the socket of the residual limb. Further disclosed is a method wherein the end pad is implanted at least partially into a residual limb by way of a surgical procedure.

BRIEF DESCRIPTION OF THE DRAWINGS

The drawings that accompany the following detailed description can be briefly described as follows:

FIG. 1 illustrates a prior art artificial limb receiving a residual limb;

FIG. 2 illustrates an artificial limb receiving a residual limb having an example end pad;

FIG. 3A is an anterior view of the FIG. 2 end pad;

FIG. 3B is representative of either a lateral or medial view of the FIG. 3A end pad;

FIG. 3C is a representative cross sectional view at line C-C showing an example of how an amputated bone attaches to the disclosed end pad;

FIG. 4A is an anterior view of another example end pad that may be used with transtibial amputees;

FIG. 4B is a superior view of the end pad of FIG. 4A;

FIG. 4C is a lateral view of the end pad of FIG. 4A;

FIG. 4D is an inferior view of the end pad of FIG. 4A;

FIG. 5A is an anterior view of yet another example end pad that may be used with transfemoral amputees;

FIG. 5B is a lateral view of the end pad of FIG. 5A;

FIG. 5C is a medial view of the end pad of FIG. 5A;

FIG. 5D is a posterior view of the end pad of FIG. 5A;

FIG. 6A is a superior view of yet another example end pad that may be used with transradial or transhumeral amputees;

FIG. 6B is a lateral view of the end pad of FIG. 6A;

FIG. 6C is an inferior view of the end pad of FIG. 6A;

FIG. 7 is representative of another example end pad having a spacer intermediate the end pad and an amputated bone;

FIG. 8 is representative of yet another example end pad having a liner intermediate the end pad and an amputated bone;

FIG. 9A is a front view of another example end pad;

FIG. 9B is a rear view of the FIG. 9A end pad; and

FIG. 9C is a top view of the FIG. 9A end pad.

DETAILED DESCRIPTION

FIG. 2 is representative of a residual limb 10, including an amputated bone 12 and various soft tissue 14. In most examples, an artificial limb 16 is custom-fit for the particular residual limb 10, such that the socket 18 is sized to receive the residual limb 10.

In the example shown, an end pad 20 is received over an end of the amputated bone 12. The perimeter of the end pad 20 is generally shaped to correspond to the socket 18. As will be appreciated from the below, the term “correspond” as used herein means that at least a portion of the contour of the end pad 20 is shaped in a manner that mimics at least a portion of the curvature of an expected socket 18, such that the end pad 20 provides a desired fit with the socket 18.

In one example, the end pad 20 is implanted within the soft tissue 14 directly adjacent to the amputated bone 12. When the artificial limb 16 is attached to the residual limb 10, the socket 18 receives at least some of the end pad 20. As shown, the example end pad 20 is encapsulated within the soft tissue 14. In another example, a portion of the end pad 20 is exposed. Still, in further examples, the end pad 20 may be exposed such that the end pad 20 can directly engage the socket 18. Attachment features could be provided between the end pad 20 and the socket 18 in this case, to provide a desired fit between the end pad 20 and the socket 18. Such attachment features include placing padding (such as a sleeve) between the end pad 20 and the socket 18, or placing some type of fastener between the end pad 20 and the socket 18.

FIGS. 3A-3B show the end pad 20 in further detail. For example, the end pad 20 generally includes a bone attachment portion 22 and an end portion 24 opposite the bone attachment portion 22. The bone attachment portion 22 has a recess 26 for receiving the amputated bone 12. The recess 26 may be defined between proximal (or inner, relative to the center C of the end pad 20) medial and lateral surfaces 28 p, 30 p as well as a base surface 32, and the proximal anterior and posterior surfaces 34 p, 36 p.

The lower end portion 24 may extend a distance D1, which can be as much as 25 mm (approximately 0.98 in) or 50 mm (approximately 1.97 in), below the bone attachment portion 22 (or, as shown, below the base surface 32), and is semi-spherical having an convex outer contour 40 generally defined by a radius R at an inferior surface 42 thereof. The radius R is selected to correspond to the concavity of the socket 18 and to encapsulate the end of the amputated bone 12. While the lower end portion 24 is shown as being semi-spherical, the shape of the lower end portion 24 can be varied to correspond to different sockets 18.

In the example shown, the distal (or outer) surface of the end pad 20 smoothly and continuously extends from its inferior surface 42 to its superior surface 44. The exterior of the end pad 20 is further defined by distal (or outer, relative to the center C of the end pad 20) medial, lateral, anterior and posterior surfaces 28 d, 30 d, 34 d, 36 d, respectively.

The end pad 20 may be implanted surgically by way of a surgeon attaching the end pad 20 to the amputated bone 12 immediately following amputation. This may be desirable, as the end pad 20 can be attached without requiring a patient to undergo multiple surgeries. However, the end pad 20 can be implanted post-amputation with a separate surgery.

In either case, an example surgical procedure would involve a surgeon displacing the soft tissue 14 to sufficiently expose the bone 12. The surgeon may essentially “trim” the distal end 38 of the amputated bone 12 so that it continuously engages the base surface 32. The recess 26 of the end pad 20 receives the end of the amputated bone 12. A surgical adhesive A is then used to bond the amputated bone 12 to the end pad 20, as shown in FIG. 3C. The surgical adhesive A may be MediSil, for example, or another known surgical adhesive or gel. While the example end pad 20 is attached directly adjacent the amputated bone 12 via the surgical adhesive A, the end pad 20 could be indirectly attached to the amputated bone 12, by way of an intermediate spacer S or liner L, as examples (represented in FIGS. 7-8). In yet another example, the end pad 20 could be held exclusively with soft tissue 14 completely independent from the amputated bone 12 or any bone.

It is further contemplated, within the scope of this disclosure, that an implanted end pad 20 could be removed and replaced with another end pad of another size. For example, in the case where atrophy of the soft tissue 14 causes an undesirable fit between the end pad 20 and the socket 18 of the artificial limb 16, the end pad 20 can be replaced with an end pad larger in size. The end pad 20 could also, in another example, be resizable by way of the injection or removal of medical grade fluid (such as silicone).

FIGS. 4A-4D, 5A-5D and 6A-6C show three embodiments of the end pad 20, as generally explained below. Numerals in these three embodiments generally relate to those from FIGS. 3A-3B, above, however they include a preappended “1,” “2,” or “3.”

With reference to FIGS. 4A-4D, the end pad 120 in this example is for use with transtibial, or below the knee, amputees. Due to the nature of a below the knee amputation, the distal and proximal medial and lateral surfaces 128 d, 128 p, 130 d, 130 p are generally mirror images of one another about the center C of the end pad 120 (e.g., the medial and lateral surfaces are substantially the same size and shape).

FIGS. 5A-5D show an end pad 220 adapted for use with transfemoral, or above the knee, amputees. Notably, in this example, the distal and proximal lateral surfaces 230 d, 230 p are more pronounced than the distal and proximal medial surface 228 d, 228 p. Whereas in the FIGS. 4A-4D example an even distribution of surgical adhesive A may be preferred, in this example, due to the inherent stresses and forces on a transfemoral amputee, the majority of the surgical adhesive A is desired between the amputated bone 212, and the proximal lateral and proximal anterior surfaces 230 p, 234 p.

FIGS. 6A-6C are representative of an end pad 320 for transradial (below the elbow) or transhumeral (above the elbow) amputees. In this instance, it is desired to apply the majority of the surgical adhesive A between the amputated bone 312 and proximal superior surface 344 p so that the most padding is provided at the distal superior surface 344 d. As in the example of FIGS. 4A-4D, the medial and lateral surfaces 328, 330 are generally mirror images of one another. Notably, in this example, the socket 18 of an artificial limb 10 (in this case an arm), would attach to the distal posterior surface 334 d, unlike in the prior two examples where it would attach to the inferior surface 42.

FIGS. 9A-C show another example end pad 420. The numerals in FIGS. 9A-9C correspond to those in FIGS. 3A-3C, above, with a preappended “4.” While the end pads 120, 220, and 320 are each shaped to correspond to a particular residual limb 112, 212, 312, the end pad 420 may be “universal,” in that it can be used with any residual limb 412. As shown, the end pad 420 is generally symmetrical about its center C, and thus its front and rear views are substantially the same (e.g., FIGS. 9A and 9B). The distal surfaces of the end pad 420 generally provide the end pad 420 with a “teardrop” shape. Similar to the above embodiments, the residual limb 412 can be received within the recess 426 (e.g., using adhesive A, as noted above). Accordingly, the disclosed end pad 20 can have a variety of shapes, including, but not limited to, those shown in the FIGS. 3A-9C.

Use of the disclosed end pad substantially absorbs shock and force on the amputee's residual limb, thereby increasing quality of life and allowing the amputee to walk and run longer with little to no pain. The end pad further reduces bone spurs in the amputated bone, and may restore bone canal pressure inside the amputated bone.

The disclosed end pad may be made of one or more appropriate materials including any number of medical grade silicones, polyurethanes, thermoplastic elastomers (TPEs), ultra high molecular weight polyethylenes (UHMWPEs), or polyetheretherketones (PEEKs) to name a few. The end pad could be formed of an appropriate hybrid biomaterial combination. At any rate, the selected material provides the amputee with adequate shock and force absorption, as noted above.

Terms such as “distal,” “proximal,” “anterior,” “posterior,” “superior,” “inferior,” “lateral,” and “medial” are to be construed as they would by one of ordinary skill in this art to the extent they are not otherwise defined herein. Often, in the medical field, these terms are used relative to the center of the human body. However, at certain points in this disclosure, these terms are used with reference to the center of the end pad itself, because the end pad can be used on various limbs on either side of the body. These terms are not limiting, however, and are merely used to aid in describing the structure of the various example end pads disclosed. For example, the terms “lateral” and “medial” are used to distinguish the different sides of the end pad, and are not meant to imply any specific orientation of the end pad relative to the human body.

Although the different examples have the specific components shown in the illustrations, embodiments of this invention are not limited to those particular combinations. It is possible to use some of the components or features from one of the examples in combination with features or components from another one of the examples.

One of ordinary skill in this art would understand that the above-described embodiments are exemplary and non-limiting. That is, modifications of this disclosure would come within the scope of the claims. Accordingly, the following claims should be studied to determine their true scope and content. 

1. An implantable end pad, comprising: a bone attachment portion of the end pad having a recess configured to receive an amputated bone of a residual limb; and an end portion of the end pad having a contour corresponding to at least a portion of a socket of an artificial limb.
 2. The implantable end pad as recited in claim 1, wherein the contour is convex.
 3. The implantable end pad as recited in claim 2, wherein the contour provides an inferior surface having a semi-spherical shape.
 4. The implantable end pad as recited in claim 3, wherein the contour provides a superior surface and the contour smoothly extends from the inferior surface to the superior surface of the end pad.
 5. The implantable end pad as recited in claim 1, wherein a portion of the end pad is more pronounced than another portion of the end pad when the residual limb is provided by one of an above the knee, below the elbow, and an above the elbow amputation.
 6. The implantable end pad as recited in claim 1, wherein medial and lateral surfaces of the end pad are substantially the same size and shape.
 7. The implantable end pad as recited in claim 1, wherein the end pad is symmetrical about a central axis thereof.
 8. The implantable end pad as recited in claim 1, wherein the end portion extends below the bone attachment portion by a distance within the range of 25 mm and 50 mm.
 9. The implantable end pad as recited in claim 1, wherein the end pad is configured to support soft tissue of the residual limb.
 10. The implantable end pad as recited in claim 1, wherein the end pad is made of a medical grade silicone.
 11. The implantable end pad as recited in claim 1, wherein the end pad is made of a material selected from one of polyurethanes, thermoplastic elastomers (TPEs), ultra high molecular weight polyethylenes (UHMWPEs), and polyetheretherketones (PEEKs).
 12. An artificial limb assembly, comprising: an end pad implanted beneath soft tissue and attached to an end of an amputated bone; and an artificial limb including a socket, the end pad at least partially received in the socket.
 13. The artificial limb assembly as recited in claim 12, wherein an outer contour of the end pad is convex and corresponds to a contour of the socket.
 14. The artificial limb assembly as recited in claim 12, wherein a spacer is provided between the amputated bone and the end pad.
 15. The artificial limb assembly as recited in claim 12, wherein a liner is provided between the amputated bone and the end pad.
 16. The artificial limb assembly as recited in claim 12, wherein the end pad is attached to the amputated bone by way of a surgical adhesive.
 17. A method for implanting an end pad, comprising: displacing soft tissue surrounding an amputated bone to sufficiently expose the amputated bone; positioning an end of the amputated bone within a recess of the end pad; and securing the end pad relative to the amputated bone.
 18. The method as recited in claim 17, further comprising trimming an end of the bone that will directly interface with the end pad.
 19. The method as recited in claim 17, further comprising an amputation step to provide the amputated bone, wherein the amputation step is performed during the same surgical procedure as said displacing, positioning and affixing steps.
 20. The method as recited in claim 17, further comprising an amputation step to provide the amputated bone, wherein the amputation step is performed during a different surgical procedure from said displacing, positioning and affixing steps. 